GENE DRO1 CONTROLLING DEEP-ROOTED CHARACTERISTICS OF PLANT AND UTILIZATION OF SAME

Abstract

To provide a gene that controls the deep rooting of a plant, a transgenic plant introduced with the gene, a method for controlling the deep rooting of a plant using the gene, and such, high-resolution linkage analysis was performed for a genetic locus (Dro1 locus) capable of controlling the deep rooting of a plant, which was detected between a shallow-rooted rice cultivar IR64 and a deep-rooted rice cultivar Kinandang Patong in a large-scale segregating population. As a result, it was revealed that the gene region of Dro1 is located in a region of 6.0 kbp sandwiched between Dro1-INDEL09, which is an InDel marker, and Dro1-CAPS05, which is a CAPS marker. Furthermore, it was confirmed that a transgenic plant transformed with the Kinandang Patong-type Dro1 gene shows a significantly high ratio of deep rooting. It was also confirmed that a plant having the Kinandang Patong-type Dro1 gene is resistant to drought.

Claims

1. A DNA of any one of (a) to (e) below: (a) a DNA comprising the nucleotide sequence of SEQ ID NO: 1; (b) a DNA comprising a coding region of the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17; (c) a DNA that encodes a protein comprising the amino acid sequence of any one of SEQ ID NOs: 3, 13, and 15; (d) a DNA that hybridizes under a stringent condition to a DNA comprising the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17, and has an activity of conferring a deep rooting phenotype to a plant; or (e) a DNA that encodes a protein comprising an amino acid sequence with one or more amino acid substitutions, deletions, additions, and/or insertions in the amino acid sequence of any one of SEQ ID NOs: 3, 13, and 15, and has an activity of conferring a deep rooting phenotype to a plant.

2. The DNA of claim 1, wherein the plant is a monocotyledon.

3. The DNA of claim 2, wherein the monocotyledon is a gramineous plant.

4. The DNA of claim 3, wherein the gramineous plant is selected from the group consisting of rice, wheat, barley, rye, oat, and hatomugi, corn, millet, foxtail millet, Japanese millet, sorghum, finger millet, pearl millet, teff, sugarcane, timothy, Kentucky bluegrass, orchardgrass, Italian rye grass, perennial ryegrass, tall fescue, and Bahia grass.

5. The DNA of claim 3, wherein the gramineous plant is selected from the group consisting of rice, sorghum, and corn.

6-19. (canceled)

20. A method for producing a transformed plant, which comprises the steps of introducing into a plant cell the DNA of claim 1, and regenerating a plant from the plant cell.

21. The method of claim 20, which further comprises the step of selecting a transformed plant cell or transformed plant, which has the DNA in a single copy.

22. A method for assessing whether a plant has a deep rooting phenotype, wherein a test plant is judged to have a deep rooting phenotype when a molecular weight or nucleotide sequence is identical, and which comprises the steps of (a) to (c) below: (a) preparing a DNA sample from a test plant; (b) amplifying from the DNA sample a region comprising the DNA of claim 1; and (c) comparing the molecular weight or nucleotide sequence of the amplified DNA fragment with that of the DNA.

23. A method for assessing whether a plant has a deep rooting phenotype, wherein a test plant is judged to have a deep rooting phenotype when an amplified product is obtained, which comprises the step of carrying out PCR with a primer comprising the nucleotide sequence of SEQ ID NO: 8 and a primer comprising the nucleotide sequence of SEQ ID NO: 9 using a genomic DNA prepared from the test plant as a template.

24. A method for assessing whether a plant has a deep rooting phenotype, wherein a test plant is judged not to have a deep rooting phenotype when an amplified product is obtained, which comprises the step of carrying out PCR with a primer comprising the nucleotide sequence of SEQ ID NO: 10 and a primer comprising the nucleotide sequence of SEQ ID NO: 11 using a genomic DNA prepared from the test plant as a template.

25. A method for selecting a plant having a deep rooting phenotype, which comprises the steps of (a) and (b) below: (a) producing a cultivar by crossing an arbitrary plant with a plant having a deep rooting phenotype; and (b) assessing by the method of claim 22 whether a plant obtained in step (a) has a deep rooting phenotype.

26-28. (canceled)

29. A DNA comprising the nucleotide sequence of any one of SEQ ID NOs: 4 to 11.

30. A method for conferring a deep rooting trait to a plant, which comprises the steps of (i) and (ii) below: (i) introducing into a plant cell the DNA of claim 1 or a vector comprising the DNA; and (ii) regenerating a plant from the plant cell.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0112] FIGS. 1A-E present photographs showing assessment of each lineage for the deep rooting using an improved basket method. A ring is attached to a stainless-steel basket. The ring is arranged at a position so that the roots are judged to be deep roots when elongating at an angle of 50 degrees or deeper with respect to ground surface. In each legend, the first and second abbreviations refer to the lineage name and generation, respectively. As indicated by the legend, FIG. 1A provides IR64; FIG. 1B provides Kinandang Patong; FIG. 1C provides Dro1-NIL; FIG. 1D provides Vector Control (V43, T0); FIG. 1E provides Dro1-Transformed Lineage (D17, T0).

[0113] FIG. 2 presents a graph showing distribution of the deep rooting ratio in the T0 generation of the IR64 transformants introduced with a vector carrying Dro1 or the vector alone.

[0114] FIG. 3 presents graphs showing the relationship between the deep rooting ratio and the signal intensity (real-time PCR) according to the copy number of the transformation vector in the T1 generation of the IR64 transformants introduced with a vector carrying Dro1 or the vector alone. Single copy and multicopy refer to a lineage introduced with only a single copy of Dro1 and a lineage introduced with multiple copies of Dro1 in the T0 generation, respectively. In the T1 generation, the single-copy lineage is separated into null type (0 copy), heterozygote (one copy), and homozygote (two copies), and the signal intensities are grouped into three types according to the number of copies. However, unlike Southern analysis, real-time PCR, in principle, does not always give the same signal intensity even if the copy number is the same among plants. The abbreviation in each graph shows the lineage number for the respective clone.

[0115] FIG. 4 presents a graph showing the distributions of the deep rooting ratio in Fox lineage and Nipponbare.

[0116] FIG. 5 presents a diagram showing the result of analyzing the sorghum and corn orthologs. Dro1, rice (Kinandang Patong); SbDro1L1, sorghum ortholog of Dro1; ZmDro1L1, corn ortholog of Dro1.

[0117] FIG. 6 presents photographs showing comparison of the deep rooting of Dro1-NIL with those of IR64 and Kinandang Patong in a field. The white numeral shows the soil depth below ground surface. The white dashed line indicates an outline of the distribution area of the root system.

[0118] FIG. 7 presents a graph showing the time course of soil water potential in the experimental field for a drought resistance test. “Irregated” and “Drought” indicate the irrigation area and drought stress area, respectively. The soil depths where the water potential was monitored are shown in parentheses. At a soil depth of 25 cm in the drought stress area, a rapid progression of soil desiccation is observed about 70 days after seeding.

[0119] FIG. 8 presents photographs showing time-dependent difference in resistance to leaf rolling between IR64 and Dro1-NIL under a drought stress condition. The plant photographs are views taken from straight above. The numbers of days shown at the top of the figure are the days of stress treatment after irrigation was terminated in the drought stress area.

[0120] FIGS. 9A-E present graphs and photographs showing differences in the leaf temperature, stomatal conductance, and photosynthesis rate between IR64 and Dro1-NIL under a drought stress condition. FIG. 9A shows a visible image of rice plants 35 days after termination of irrigation. The first and second lines from right are IR64; the third and fourth are Dro1-NIL. FIG. 9B shows an image showing the temperature distribution of the rice plants 35 days after termination of irrigation (an infrared thermography image taken for the same plants as shown in FIG. 9A). The first and second lines from right are IR64; the third and fourth are Dro1-NIL. The color difference implies the following: as the color is warmer, the temperature is higher; as the color is cooler, the temperature is lower. This photograph suggests that the leaf temperature is different between IR64 and Dro1-NIL (the leaf temperature of Dro1-NIL is on average 0.7° C. lower than that of IR64). The cool colors are distributed more widely in Dro1-NIL, suggesting that the leaf temperature of Dro1-NIL is lower than that of IR64. FIG. 9C shows changes in the leaf temperature of Dro1-NIL after termination of irrigation in the drought stress area. The values are relative to the leaf temperature of IR64 and were determined by subtracting the mean leaf temperature of IR64 from that of Dro1-NIL. The leaf temperature of Dro1-NIL was found to be lower than that of IR64 at every measurement date. FIG. 9D shows difference in the stomatal conductance between IR64 and Dro1-NIL after termination of irrigation in the drought stress area. * indicates that the stomatal conductance of Dro1-NIL is significantly greater than that of IR64 at a level of 5%. FIG. 9E shows difference in the photosynthesis rate between IR64 and Dro1-NIL after termination of irrigation in the drought stress area. * indicates that the photosynthesis rate of Dro1-NIL is significantly greater than that of IR64 at a level of 5%.

[0121] FIGS. 10A and 10B present diagrams and photographs showing results of yield determination for IR64 and Dro1-NIL cultivated under a drought stress condition. FIG. 10A shows various phenotypic differences between harvested IR64 and Dro1-NIL, which were grown in the drought stress area. Vertical bar indicates standard deviation. *, **, or *** indicates that Dro1-NIL is significantly larger than IR64 at a level of 5%, 1%, or 0.1%, respectively. FIG. 10B presents photographs showing the average panicles of IR64 and Dro1-NIL harvested in the drought stress area.

[0122] FIG. 11 presents photographs showing a lateral view of the dissected experimental field for testing drought resistance, which shows differences in the root system distribution between IR64 and Dro1-NIL in a drought stress area. The upper panel for each lineage shows a sectional view of the experimental field, and the lower panel shows an enlarged image obtained by washing off the additional topsoil to observe whether the roots penetrated the gravel stratum. The arrow heads indicate roots of Dro1-NIL that have penetrated the gravel stratum. It is shown that in IR64, there was no root that penetrated the gravel stratum and reached the deeper layer, but in Dro1-NIL, many roots penetrated the gravel stratum and reached the deeper layer.

[0123] FIG. 12 presents a graph showing the time course of water potential in the field soil.

[0124] FIG. 13 presents photographs showing the appearance of plants 120 days after seeding in field areas with or without fertilization. The upper panels show the overall view including the respective areas. The lower panels are photographs taken from above as enlarged images of the respective areas. In IR64, leaf rolling is observed both in the areas with or without fertilization. Meanwhile, Dro1-NIL shows no leaf rolling.

[0125] FIG. 14 presents a photograph showing PCR marker results for assessing the Dro1 gene deletion. At each annealing temperature, the left and right lanes show the results for IR64 and Kinandang Patong, respectively.

MODE FOR CARRYING OUT THE INVENTION

[0126] The present invention provides a DNA of any one of (a) to (e) below: [0127] (a) a DNA comprising the nucleotide sequence of SEQ ID NO: 1; [0128] (b) a DNA comprising the coding region of the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17; [0129] (c) a DNA that encodes a protein comprising the amino acid sequence of any one of SEQ ID NOs: 3, 13, and 15; [0130] (d) a DNA that hybridizes under a stringent condition to a DNA comprising the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17, and has an activity of conferring a deep rooting phenotype to a plant; or [0131] (e) a DNA that encodes a protein comprising an amino acid sequence with one or more amino acid substitutions, deletions, additions, and/or insertions in the amino acid sequence of any one of SEQ ID NOs: 3, 13, and 15, and has an activity of conferring a deep rooting phenotype to a plant.

[0132] Hereinafter, occasionally, the above-described DNAs are also referred to as “DNA of the present invention” or “Dro1 gene”. Meanwhile, a protein encoded by a DNA of the present invention is sometimes referred to as “protein of the present invention” or “Dro1 protein”.

[0133] Herein, “comprise” also refers to both “comprise” and “consist of”.

[0134] Meanwhile, the DNA of (e) above can also be referred to as: [0135] (e) a DNA encoding a protein having at least a mutation selected from one or more amino acid substitutions, deletions, additions, and insertions in the amino acid of any one of SEQ ID NOs: 3, 13, and 15, and having the activity of conferring a deep rooting trait to a plant.

[0136] Furthermore, a DNA of the present invention can be referred to as “isolated DNA”.

[0137] The genomic DNA nucleotide sequence for the Dro1 gene of rice cultivar Kinandang Patong is shown in SEQ ID NO: 1; the nucleotide sequence of the cDNA is shown in SEQ ID NO: 2; and the amino acid sequence of the protein encoded by the coding regions of the nucleotide sequences (Dro1 protein) is shown in SEQ ID NO: 3.

[0138] The protein-encoding region in the nucleotide sequence of SEQ ID NO: 1 consists of the nucleotides at positions 264 to 2,685.

[0139] Meanwhile, the protein-encoding region in the nucleotide sequence of SEQ ID NO: 2 consists of the nucleotides at positions 264 to 1019.

[0140] Furthermore, the nucleotide sequence of the Dro1 gene and its upstream including the promoter region of Kinandang Patong is shown in SEQ ID NO: 17. When compared to the sequence of the equivalent region in Nipponbare (SEQ ID NO: 18), the sequence in Kinandang Patong (SEQ ID NO: 17) contains a single-nucleotide substitution and a deletion of 30 nucleotides about 1.2 kb upstream of the Dro1 gene. Specifically, “T” of the “GATA” motif (the nucleotide at position 6 in the nucleotide sequence of SEQ ID NO: 18) in Nipponbare is substituted with “G” in Kinandang Patong (the nucleotide at position 6 in the nucleotide sequence of SEQ ID NO: 17). In addition, the 30 nucleotides at positions 7 to 36 in SEQ ID NO: 18 are deleted in the corresponding region of Kinandang Patong.

[0141] The nucleotide sequence of the coding sequence (CDS) in the sorghum-derived Dro1 gene is shown in SEQ ID NO: 12, while the amino acid sequence of the protein encoded by the coding region of the nucleotide sequence is shown in SEQ ID NO: 13.

[0142] The protein coding region of the nucleotide sequence of SEQ ID NO: 12 (CDS sequence) consists of the nucleotides at positions 1 to 789.

[0143] The nucleotide sequence of CDS in the corn-derived Dro1 gene is shown in SEQ ID NO: 14, while the amino acid sequence of the protein encoded by the coding region of the nucleotide sequence is shown in SEQ ID NO: 15.

[0144] The protein coding region of the nucleotide sequence of SEQ ID NO: 14 (CDS sequence) consists of the nucleotides at positions 1 to 768.

[0145] The Dro1 gene of the present invention has the activity of conferring a deep rooting trait to a plant. Herein, the “deep rooting trait” refers to the nature that the root, an underground organ of plant, extends in soil with a deep angle relative to ground surface. Herein, “a deep angle” means that the angle of a root with respect to ground surface is at least 50°, preferably 60°, more preferably 70°, and yet more preferably 80° or more.

[0146] Whether a DNA has the activity of conferring a deep rooting trait to a plant can be confirmed by preparing a plant transformed with the Dro1 gene and determining the angle of the plant relative to ground surface. Plants can be assessed for the angle relative to ground surface, for example, by the basket method and an improved basket method described in the Examples herein as well as by the trench method, monolith method, and core sampling method; however, such methods are not limited thereto.

[0147] DNAs encoding a Dro1 protein of the present include genomic DNAs, cDNAs, and chemically-synthesized DNAs. Such genomic DNAs and cDNAs can be prepared by conventional methods known to those skilled in the art. The genomic DNAs can be prepared, for example, as follows. Genomic DNA is extracted from plants of a rice cultivar (for example, Kinandang Patong), sorghum, or corn having a deep rooting to prepare a genomic library (vectors such as plasmids, phages, cosmids, BACs, and P1 artificial chromosomes (PACs) can be used, but are not limited thereto); and the library is amplified, and screened by colony or plaque hybridization using a probe prepared from a DNA encoding Dro1 protein (for example, DNA having the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17). Alternatively, such genomic DNAs can be prepared by PCR using primers prepared to be specific to a DNA encoding Dro1 protein (for example, DNA comprising the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17). Meanwhile, the cDNAs can be prepared, for example, as follows. cDNA is synthesized using mRNA extracted from plants of a rice cultivar (for example, Kinandang Patong) having a deep rooting, and inserted into a vector such as ,ZAP to construct a cDNA library; and the library is amplified and screened by colony or plaque hybridization. Alternatively, the cDNAs can be prepared by PCR in the same manner described above.

[0148] On the other hand, the chemically-synthesized DNAs can be prepared, for example, by using oligonucleotide synthesizers available on the market.

[0149] Alternatively, DNAs encoding a Dro1 protein of the present invention can be prepared by extracting genomic DNA or mRNA from sorghum (for example, leaf blade and sheath) or corn (for example, leaf blade and sheath) having a deep rooting.

[0150] The present invention comprises DNAs that encode a protein functionally equivalent to the Dro1 protein of any one of SEQ ID NOs: 3, 13, and 15. Herein, “functionally equivalent to Dro1 protein” means that the protein of interest has a function of conferring a deep rooting trait to a plant. The preferred DNAs are those derived from monocotyledons, more preferably those derived from the Gramineae family, Liliaceae family, Bromeliaceae family, Palmae family, Araceae family, Zingiberaceae family, and Orchidaceae family, still more preferably those derived from rice, wheat varieties (wheat, barley, rye, oat, and Job's tears (hatomugi)), corn, millet, foxtail millet, Japanese millet, sorghum, finger millet, pearl millet, teff, sugarcane, timothy, Kentucky bluegrass, orchardgrass, Italian ryegrass, perennial ryegrass, tall fescue, and Bahia grass, and particularly preferably those derived from rice, sorghum, and corn.

[0151] Such DNAs include, for example, mutants, derivatives, alleles, variants, and homologs that encode a protein having the function to confer a deep rooting trait to a plant and comprising an amino acid sequence with one or more (for example, 2, 3, 4, 5, 10, 20, 30, 40, 50, or 100 residues) amino acid substitutions, deletions, additions, and/or insertions in the amino acid sequence of any one of SEQ ID NOs: 3, 13, and 15.

[0152] Examples of methods well-known in the art for preparing DNAs encoding a protein with altered amino acid sequence include site-directed mutagenesis methods (Kramer, W. and Fritz, H.-J. (1987) Oligonucleotide-directed construction of mutagenesis via gapped duplex DNA. Methods in Enzymology, 154: 350-367). In nature, mutations in nucleotide sequences may also lead to mutations in the amino acid sequences of proteins encoded thereby. As described above, DNAs encoding a protein having an amino acid sequence with one or more amino acid substitutions, deletions, or additions in the amino acid sequence encoding the naturally-occurring Dro1 protein are included in the DNAs of the present invention, as long as they encode a protein having the function equivalent to the naturally-occurring Dro1 protein (amino acid sequence of any one of SEQ ID NOs: 3, 13, and 15). Such DNAs include, for example, DNAs comprising the nucleotide sequence of SEQ ID NO: 16. The DNAs comprising the nucleotide sequence of SEQ ID NO: 16 have a nucleotide sequence with a 1-bp addition at each of the 5′ and 3′ ends in a DNA comprising the nucleotide sequence of SEQ ID NO: 2. The DNAs also have a substitution of G for A at bp position 373 from the 5′ end (at bp position 372 from the 5′ end in SEQ ID NO: 2). Because of this nucleotide substitution, the amino acid sequence encoded by such a DNA comprising the nucleotide sequence of SEQ ID NO: 16 has a non-synonymous amino acid substitution of glutamic acid for lysine at position 37 in the amino acid sequence of SEQ ID NO: 3. The present invention also provides such proteins comprising an amino acid sequence with a substitution of glutamic acid for lysine at position 37 in the amino acid sequence of SEQ ID NO: 3. The present invention also provides DNAs encoding such a protein (for example, DNAs comprising the nucleotide sequence of SEQ ID NO: 16).

[0153] Even if the nucleotide sequence has a mutation, in some cases, the mutation may not result in any mutations in the amino acid sequence of the protein (mutation degeneracy). Such mutants (degenerate mutants) are also included in the DNAs of the present invention.

[0154] Other methods well known to those skilled in the art for preparing a DNA encoding a protein functionally equivalent to the Dro1 protein of any one of SEQ ID NOs: 3, 13, and 15 include methods using hybridization techniques (Southern, E. M. (1975) Journal of Molecular Biology, 98, 503) or PCR techniques (Saiki, R. K. et al., (1985) Science, 230, 1350-1354; Saiki, R. K. et al., (1988) Science, 239, 487-491). Specifically, those skilled in the art can readily isolate DNAs with high homology to the Dro1 gene from rice or other plants using as a probe the nucleotide sequence of the Dro1 gene (the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17) or a portion thereof, or using as primers oligonucleotides that specifically hybridize to the Dro1 gene (the nucleotide sequence of any one of SEQ ID NOs: 1, 2, 12, 14, 16, and 17). The DNAs of the present invention also comprise such DNAs encoding a protein that is functionally equivalent to the Dro1 protein, which can be isolated by using hybridization or PCR techniques.

[0155] To isolate such DNAs, a hybridization reaction is preferably carried out under stringent conditions. Those skilled in the art can appropriately select stringent hybridization conditions. For example, pre-hybridization is carried out in a hybridization solution containing 25% formamide or 50% formamide under more stringent conditions, and 4×SSC, 50 mM Hepes (pH 7.0), 10× Denhardt's solution, and 20 μg/ml denatured salmon sperm DNA at 42° C. overnight; then labeled probes are added, and hybridization is carried out by incubation at 42° C. overnight. Post-hybridization washing can be carried out with the following conditions for the wash solution and temperature: for example, “2×SSC, 0.1% SDS, 50° C.”, “2×SSC, 0.1% SDS, 42° C.”, “lx SSC, 0.1% SDS, 37° C.”, or so; “2×SSC, 0.1% SDS, 65° C.”, “0.5×SSC, 0.1% SDS, 42° C.”, or so for a more stringent condition; and “0.2×SSC, 0.1% SDS, 65° C.” or so for an even more stringent condition. As the stringency of the hybridization increases, isolation of DNAs with high homology to the probe sequence is expected. However, the above-described combinations of SSC, SDS, and temperature conditions are mere examples, and those skilled in the art can achieve similar stringencies as those described above by appropriately combining the above or other elements (such as probe concentration, probe length, or hybridization reaction time) which determine the stringency of hybridization.

[0156] Thus, the protein encoded by such an isolated DNA is expected to have high homology to the amino acid sequence of Dro1 protein (SEQ ID NO: 3, 13, or 15) at the amino acid level. Furthermore, the DNA is expected to have high homology to the nucleotide sequence of a DNA encoding Dro1 protein (SEQ ID NO: 1, 2, 12, 14, 16, or 17) at the nucleotide sequence level. The high homology refers to a sequence identity of at least 50% or more, preferably 70% or more, more preferably 90% or more (for example, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more) over the entire amino acid or nucleotide sequence. Such amino acid sequence or nucleotide sequence identity can be determined using the BLAST algorithm by Karin and Altschul (Proc. Natl. Acad. Sci. USA 87: 2264-2268, 1990; Proc Natl Acad Sci USA 90: 5873, 1993). Programs called BLASTN and BLASTX have been developed based on the BLAST algorithm (Altschul S F, et al., J Mol Biol 215: 403, 1990). When nucleotide sequences are analyzed using BLASTN, parameters may be set at: score=100 and wordlength=12, for example. Alternatively, when amino acid sequences are analyzed using BLASTX, parameters may be set at: score=50 and wordlength=3, for example. When the BLAST and Gapped BLAST programs are used, it is possible to use default parameters for each program. Specific procedures are known for these analytical methods.

[0157] The DNAs of the present invention can be used, for example, in preparing recombinant proteins and producing plant transformants having a deep rooting trait.

[0158] Recombinant proteins are typically prepared by inserting DNAs encoding proteins of the present invention into appropriate expression vectors, introducing the vectors into appropriate cells, culturing the transformed cells, and purifying the expressed proteins. Recombinant proteins can be expressed as fusion proteins with other proteins to make purification easier, for example, as fusion proteins with maltose-binding protein using Escherichia coli as a host (New England Biolabs, USA, vector pMAL series), as fusion proteins with glutathione S-transferase (GST) (Amersham Pharmacia Biotech, vector pGEX series), or tagged with histidine (Novagen, pET series). The host cells are not particularly limited, so long as the cell is suitable for expressing the recombinant proteins. It is possible to use, for example, yeast, various plant or animal cells, insect cells or such in addition to the above-described E. coli. Vectors can be introduced into host cells by a variety of methods known to those skilled in the art. For example, introduction methods using calcium ions can be used for introduction into E. coli (Mandel, M. & Higa, A. (1970) Journal of Molecular Biology, 53, 158-162; Hanahan, D. (1983) Journal of Molecular Biology, 166, 557-580). Recombinant proteins expressed in the host cells can be purified and recovered from the host cells or a culture supernatant thereof by methods known to those skilled in the art. Recombinant proteins can be easily purified by affinity when expressed as fusion proteins with the above-described maltose-binding protein or such. Alternatively, plant transformants introduced with a DNA of the present invention may be produced by the techniques described herein below. The proteins of the present invention can be prepared from such plants. Accordingly, the plant transformants of the present invention include plants introduced with a DNA of the present invention to prepare a protein of the present invention as well as plants introduced with a DNA of the present invention to confer a deep rooting trait to plants, which are described herein below.

[0159] The resulting recombinant protein can be used to prepare antibodies that bind to the protein. Polyclonal antibodies can be prepared, for example, as follows. Animals for immunization such as rabbits are immunized with a purified protein of the present invention or a partial peptide thereof; and after a certain period, their blood is collected, and clotted blood is removed. Meanwhile, monoclonal antibodies can be prepared as follows. Myeloma cells are fused with antibody-producing cells from animals immunized with an above-described protein or peptide; single clone cells (hybridomas) producing the antibody of interest are isolated; and the antibody is obtained from the cells. The resulting antibody can be used to purify or detect proteins of the present invention. The present invention comprises antibodies that bind to a protein of the present invention. Such antibodies can be used to detect expression sites of the Dro1 protein in plants or to assess whether a plant species expresses the Dro1 protein. For example, the amino acid sequence from positions 227 to 251 of the Kinandang Patong-type Dro1 protein is a sequence characteristic of cultivars having a deep rooting trait. Thus, antibodies that specifically recognize the entire amino acid sequence or a portion thereof can be used to assess whether a plant species expresses the Kinandang Patong-type Dro1 protein (whether it has a deep rooting trait).

[0160] The present invention also provides vectors and transformed cells comprising the Dro1 gene.

[0161] With regard to the vectors of the present invention, for example, when the host is E. coli, as long as the vector has an “ori” for amplification in E. coli, such that vectors are amplified and prepared in large quantities in E. coli (for example, JM109, DH5α, HB101, and XL1Blue) or such, and further has a selection gene for transformed E. coli (for example, a drug resistance gene that allows discrimination using a drug (ampicillin, tetracycline, kanamycin, chloramphenicol, or such)), the vectors are not limited. Such vectors include, for example, M13 vectors, pUC vectors, pBR322, pBluescript, and pCR-Script. In addition to the above vectors, for example, pGEM-T, pDIRECT, and pT7 can also be used for the subcloning and excision of cDNAs. When using vectors to produce the Dro1 protein, expression vectors are particularly useful. When an expression vector is expressed in E. coli, for example, it should have the above characteristics in order to be amplified in E. coli. Additionally, when E. coli such as JM109, DH5α, HB101, or XL1-Blue are used as the host, the vector must have a promoter that allows efficient expression in E. coli, for example, a lacZ promoter (Ward et al. Nature 341: 544-546, 1989; FASEB J. 6: 2422-2427, 1992), araB promoter (Better et al. Science 240:1041-1043, 1988), or T7 promoter. Other examples of the vectors include pGEX-5X-1 (Pharmacia), “QlAexpress system” (QIAGEN), pEGFP, and pET.

[0162] Furthermore, the vector may comprise a signal sequence for polypeptide secretion. When producing polypeptides into the periplasm of E. coli, the pelB signal sequence (Lei, S. P. et al. J. Bacteriol. 169: 4379 (1987)) may be used as a signal sequence for polypeptide secretion. For example, calcium chloride methods or electroporation methods may be used to introduce the vector into a host cell. Vectors for expressing in the plant body include pMH1, pMH2, pCAMBIA, and such.

[0163] In addition to E. coli, expression vectors derived from mammals (e.g., pcDNA3 (Invitrogen), pEGF-BOS (Nucleic Acids Res. 18(17): 5322 (1990)), pEF, and pCDM8), insect cells (e.g., “Bac-to-BAC baculovirus expression system” (GIBCO-BRL) and pBacPAK8), plants (e.g., pMH1 and pMH2), animal viruses (e.g., pHSV, pMV, and pAdexLcw), retroviruses (e.g., pZIPneo), yeasts (e.g., “Pichia Expression Kit” (Invitrogen), pNV11 and SP-Q01), and Bacillus subtilis (e.g., pPL608 and pKTH50) may also be used as vectors for producing the Dro1 protein.

[0164] For expression in animal cells such as CHO, COS, and NIH3T3 cells, the vector must have a promoter necessary for expression in such cells, for example, an SV40 promoter (Mulligan et al. Nature 277: 108 (1979)), MMLV-LTR promoter, EF1α promoter (Mizushima et al. Nucleic Acids Res. 18: 5322 (1990)), or CMV promoter. It is even more preferable that the vector comprises a gene for selecting transformants (for example, a drug-resistance gene enabling discrimination by a drug (such as neomycin and G418)). Examples of vectors with such characteristics include pMAM, pDR2, pBK-RSV, pBK-CMV, pOPRSV, and pOP13.

[0165] The transformed cells of the present invention can be used, for example, as a production system for expressing or producing proteins of the present invention. Such protein production systems include in vitro and in vivo systems.

[0166] When eukaryotic cells are used, for example, animal cells, plant cells, or fungal cells are used as host cells. Known animal cells include mammalian cells (for example, cells such as 3T3, myeloma cells, BHK (baby hamster kidney), HeLa, and Vero, in addition to CHO cells, COS cells, and NIH3T3 cells described above), amphibian cells (for example, Xenopus laevis oocytes (Valle, et al., Nature (1981) 291, 358-340)), and insect cells (for example, cells such as sf9, sf21, and Tn5). Among CHO cells, dhfr-CHO (Proc. Natl. Acad. Sci. USA (1980) 77, 4216-4220), which is DHFR gene-deficient CHO cells, and CHO K-1 (Proc. Natl. Acad. Sci. USA (1968) 60, 1275) can be preferably used in the present invention. CHO cells are particularly preferred for use in large-scale expression.

[0167] Plant cells include, for example, plant-derived cells described below as wells as Nicotiana tabacum-derived cells known as a protein production system. It is possible to culture calluses from cells.

[0168] Meanwhile, fungal cells include yeast cells, for example, cells of the genus Saccharomyces, for example, Saccharomyces cerevisiae; cells of filamentous fungi, for example, the genus Aspergillus, for example, Aspergillus niger, but are not limited thereto.

[0169] The present invention also provides the above-described cells introduced with a DNA or vector of the present invention.

[0170] Furthermore, the present invention relates to plants transformed with the Dro1 gene, which have a deep rooting trait.

[0171] Whether a plant has a deep rooting trait can also be assessed by comparing it with a control. Herein, as long as the root of plant transformant extends in soil at a deeper angle with respect to ground surface when compared to a control, even if the angle difference is very small, the transformant is judged to “have a deep rooting trait”. Whether a root of a plant transformant extends in soil with a deeper angle with respect to ground surface can be assessed by the methods described above.

[0172] Herein, “control” refers to a plant that is of the same type as a plant transformant of the present invention, but without artificial introduction of a DNA of the present invention or which does not have any DNA of the present invention. Herein, the control is not particularly limited, as long as it is a plant that is of the same type as a plant transformant of the present invention, but without artificial introduction of a DNA of the present invention or which does not have any DNA of the present invention. Accordingly, the “control” of the present invention also comprises plants artificially introduced with DNAs other than the DNAs of the present invention. Such plants include, but are not limited to, for example, plants of the same type as a plant transformant of the present invention, which are transformed with a DNA other than the DNAs of the present invention, a DNA of the present invention introduced with a mutation that causes loss-of-function in the DNA, a DNA of the present invention converted into a type that suppresses the function, or a DNA fragment containing only a portion of a DNA of the present invention which is insufficient for exerting the function of the DNA.

[0173] Plants transformed with a DNA of the present invention are not particularly limited as long as they have a deep rooting trait, and may contain modifications in any other parts. Such modifications in any other parts include, for example, morphological changes of panicles, but are not limited thereto.

[0174] Plant transformant can be prepared using a DNA of the present invention by the following procedure. The DNA or a vector inserted with the DNA is introduced into plant cells. Then, plants are regenerated from the resulting transformed plant cells.

[0175] In the present invention, preferred vectors are those capable of expressing inserted genes in plant cells, and include the vectors described above (for example, vectors such as pMH1, pMH2, and pCAMBIA vector); however, the vectors are not particularly limited. The vectors of the present invention may comprise, for example, a promoter (for example, Cauliflower mosaic virus 35S promoter) for constitutive gene expression in plant cells. When such a promoter is used, a DNA is designed so that a DNA of the present invention is operably linked downstream of the promoter. Then, a designed vector comprising the DNA is introduced into plant cells. Plant transformants expressing the DNA of the present invention can be obtained by regenerating the resulting transformed plant cells. Thus, the present invention also provides DNAs to which a DNA of the present invention is operably linked downstream of a promoter. Herein, “operably linked” means that a promoter sequence is linked to a DNA of the present invention so that the expression of the DNA is induced upon binding of transcriptional factors to the promoter sequence.

[0176] It is possible to use, in addition to the above, vectors with a promoter that is activated upon extrinsic stimulation in an inducible manner.

[0177] The plant species into which the aforementioned DNAs or vectors are introduced are not particularly limited and include, for example, monocotyledons. Monocotyledons include, but are not limited to, plants belonging to the Gramineae family, Liliaceae family, Bromeliaceae family, Palmae family, Araceae family, Zingiberaceae family, and Orchidaceae family. Plants belonging to the Gramineae family include, but are not limited to, rice, wheat varieties (wheat, barley, rye, oat, and Job's tears (hatomugi)), corn, millet, foxtail millet, Japanese millet, sorghum, finger millet, pearl millet, teff, sugarcane, timothy, Kentucky bluegrass, orchardgrass, Italian ryegrass, perennial ryegrass, tall fescue, and Bahia grass.

[0178] Plant cells into which the aforementioned DNAs or vectors are introduced are not particularly limited and may be in any form as long as they can be used to regenerate plants. For example, suspension-cultured cells, protoplasts, leaf sections, calli, and germinated seed can be used.

[0179] Introduction of the aforementioned DNAs or vectors into plant cells can be performed using methods known to one skilled in the art, such as polyethylene glycol methods, electroporation, Agrobacterium-mediated methods, and particle gun methods. In the Agrobacterium-mediated methods, for example, according to the method by Nagel et al. (Nagel, R. et al. FEMS Microbiol. Lett. 67, 1990, 325-328), a DNA can be introduced into plant cells by introducing into Agrobacteria an expression vector to which the DNA is inserted, and infecting plant cells with the Agrobacteria via direct infection or by the leaf disc method. The above-mentioned vector comprises an expression promoter so that, for example, the DNA of the present invention is expressed in a plant after introduction into the plant. Generally, the DNA of the present invention is located downstream of the promoter, and a terminator is located further downstream of such a DNA. The recombinant vector used for this purpose is suitably selected by one skilled in the art, depending on the type of plant or method of introduction.

[0180] The above-mentioned promoters include, for example, the CaMV35S derived from cauliflower mosaic virus and the ubiquitin promoter from corn (JP-A (Kokai) H02-79983).

[0181] Examples of the above-mentioned terminator can be a terminator derived from cauliflower mosaic virus and the terminator from the nopaline synthase gene; however, the promoter and terminator are not limited thereto, as long as they function in a plant.

[0182] Regeneration of a plant from a plant cell can be carried out according to the type of plant by methods known to those skilled in the art. Examples include the following methods, but are not limited thereto: [0183] for rice, the method of Fujimura et al. (Fujimura. et al. Tissue Culture Lett. 2, 1995, 74); [0184] for wheat, the method of Harris et al. (Harris, R. et al. Plant Cell Reports. 7, 1988, 337-340) and [0185] the method of Ozgen et al. (Ozgen, M. et al. Plant Cell Reports. 18, 1998, 331-335); [0186] for barley, the method of Kihara and Funatsuki (Kihara, M. and Funatsuki, H. Breeding Sci. 44, 1994, 157-160) and the method of Lurs and Lorz (Lurs, R. and Lorz, H. Theor. Appl. Genet. 75, 1987, 16-25); [0187] for corn, the method of Shillito et al. (Shillito, R. D., et al. Bio/Technology, 7, 1989, 581-587) and the method of Gordon-Kamm et al. (Gordon-Kamm, W. J. et al. Plant Cell. 2(7), 1990, 603-618); [0188] for sorghum, the method of Wen et al. (Wen, F. S., et al. Euphytica. 52, 1991, 177-181) and the method of Hagio (Hagio, T. Breeding Sci. 44, 1994, 121-126); [0189] for rye, the method of Castillo et al. (Castillo A. M., Vasil V., Vasil I. K. (1994) Nature Biotechnology 12: 1366-1371.); [0190] for oat, the method of Cho et al. (Cho M. J., WEN J., LEMAUX P. G., (1999) Plant science 148: 9-17.); [0191] for pearl millet, the method of O'Kennedy et al. (O'Kennedy M. M., Burger J. T., Botha F. C. (2004) Plant Cell Reports 22: 684-690.); [0192] for Kentucky bluegrass, the method of Ha et al. (Ha C. D., Lemaux P. G., Cho M. J. (2001) In Vitro Cellular & Developmental Biology-Plant 37: 6-11.); [0193] for orchardgrass, the method of CHO et al. (CHO M. J., CHOI H. W., LEMAUX P. G. (2001) Plant cell reports 20: 318-324.); [0194] for Italian rye grass, the method of Ye et al. (Ye X., Wang Z. Y., Wu X., Potrykus I., Spangenberg G. (1997) Plant Cell Reports 16: 379-384.); [0195] for perennial ryegrass, the method of Spangenberg et al. (Spangenberg G., Wang Z. Y., Wu X., Nagel J., Potrykus I. (1995) Plant science 108: 209-217.); [0196] for tall fescue, the method of Wang et al. (Wang Z. Y., Takamizo T., Iglesias V. A., Osusky M., Nagel J., Potrykus I., Spangenberg G. (1992) Nature Biotechnology 10: 691-696.); and [0197] for Bahia grass, the method of Smith et al. (Smith R. L., Grando M. F., Li Y. Y., Seib J. C., Shatters R. G. (2002) Plant Cell Reports 20: 1017-1021.).

[0198] The plants into which the DNA of the present invention is introduced may be explants, or the DNA may be introduced into the cultured cells prepared from these plants. “Plant cells” in the present invention include, for example, plant cells of a leaf, root, stem, flower, scutellum in a seed, and immature embryo; calluses; suspension-cultured cells; and germinated seed, but are not limited thereto.

[0199] In order to efficiently select the cells transformed by introducing the DNA of the present invention, the recombinant vector is introduced into the plant cells, preferably together with a suitable selection marker gene or a plasmid vector comprising a selection marker gene. The selection marker genes used for this purpose include, for example, the hygromycin phosphotransferase gene resistant to the antibiotic hygromycin, the neomycin phosphotransferase gene resistant to kanamycin or gentamycin, and the acetyltransferase gene resistant to the herbicide phosphinothricin.

[0200] The cells into which the recombinant vector has been introduced are placed on a known selection medium containing a suitable selection agent depending on the type of introduced selection marker gene, and then cultured. In this way, the transformed plant cultured cells can be obtained.

[0201] Next, plant bodies regenerated from the transformed cells are cultured in an acclimation medium. The acclimated, regenerated plants are then grown under usual culture conditions to obtain plants having deep rooting trait, from which seeds can be obtained once they mature and bear fruit. Specifically, the present invention provides methods for producing transformed plants, which comprise steps (a) and (b) below. The present invention also provides methods for conferring a deep rooting trait to plants, which comprise steps (a) and (b) below: [0202] (a) introducing a plant cell with a DNA of the present invention (Dro1 gene) or a vector carrying the DNA (Dro1 gene); and [0203] (b) regenerating a plant from the plant cell introduced with the DNA or vector in step (a).

[0204] The above-described methods for producing transformed plants may additionally comprise the step of: [0205] (c) selecting a plant to which the deep rooting trait is conferred.

[0206] The presence of the introduced foreign DNAs in the transformed plants that are regenerated and grown in this manner can be confirmed by the known PCR method or Southern hybridization method, or by analyzing the nucleotide sequences of the DNAs in plant bodies. In this case, extraction of the DNAs from the transformed plants can be carried out according to the known method by J. Sambrook et al. (Molecular Cloning, the 2nd edition, Cold Spring Harbor Laboratory Press, 1989). When analyzing the foreign genes which are present in the regenerated plant bodies and include the DNAs of the present invention, using the PCR method, an amplification reaction is carried out using as a template the DNAs extracted from the regenerated plant bodies as mentioned above. An amplification reaction can also be performed in a reaction mixture containing as primers synthesized oligonucleotides which comprise nucleotide sequences suitably selected according to the nucleotide sequences of the DNAs of the present invention. In the amplification reaction, denaturation, annealing, and extension reactions of DNAs can be repeated several tens of times to obtain amplified products of DNA fragments comprising the DNA sequences of the present invention. By subjecting the reaction mixture comprising the amplified products, for example, to agarose electrophoresis, the various kinds of amplified DNA fragments are fractionated, thereby enabling confirmation of whether a certain DNA fragment corresponds to a DNA of the present invention.

[0207] The present invention also relates to transformed plants, which are produced by introducing the Dro1 gene or a vector carrying the Dro1 gene into plant cells, and which have a deep rooting trait. The present invention also relates to methods for producing transformed plants, which comprise the step of introducing the Dro1 gene or a vector carrying the Dro1 gene into a plant cell.

[0208] Furthermore, in a preferred embodiment of the present invention, the transformed plants include those which are produced by steps (a) to (d) below, and which have a deep rooting trait. In another preferred embodiment of the present invention, the methods for producing transformed plants include those comprising the steps of: [0209] (a) introducing the Dro1 gene or a vector carrying the Dro1 gene into a plant cell; [0210] (b) determining the copy number of the artificially introduced Dro1 gene or vector carrying the Dro1 gene in the plant cell of step (a); [0211] (c) selecting a transformed plant cell whose copy number of the artificially introduced Dro1 gene or vector carrying the Dro1 gene is one (that contains in a single copy of the gene or vector); and [0212] (d) regenerating a plant from the transformed plant cell selected in step (c).

[0213] In the methods described above, the copy numbers of the artificially introduced Dro1 gene or vector carrying the Dro1 gene in the plants may be determined to select plants in which the copy number is 1 after a plant is regenerated from the transformed plant cell comprising the Dro1 gene. Thus, the present invention relates to transformed plants which are produced by steps (a) to (c) below, and which have a deep rooting trait. The present invention also relates to methods for producing transformed plants, which comprise the steps of: [0214] (a) introducing the Dro1 gene or a vector carrying the Dro1 gene into a plant cell and regenerating a plant from the plant cell; [0215] (b) determining the copy number of the artificially introduced Dro1 gene or vector carrying the Dro1 gene in the plant of step (a); and [0216] (c) selecting a transformed plant whose copy number of the artificially introduced Dro1 gene or vector carrying the Dro1 gene is one.

[0217] Introduction of the Dro1 gene or a vector carrying the Dro1 gene into plant cells and plant regeneration from the transformed plant cells can be achieved by the methods described above. Meanwhile, the copy number of the Dro1 gene or vector carrying the Dro1 gene in transformed plant cells or transformed plants can be determined, for example, by Southern blot analysis, real-time PCR method, nucleotide sequence analysis, or the like. However, such methods are not limited to these examples.

[0218] Herein, “copy number” refers to the number of Dro1 genes or vectors carrying the gene introduced into plants by transformation. Specifically, herein, “copy number” does not include the number of endogenous Dro1 genes in the plants (endogenous genes).

[0219] As described in the Examples herein, the present inventors produced plants of T1 generation from transformed plants (T0 generation) in which the copy number of the artificially introduced Dro1 gene is 1, and checked the relation between the deep rooting ratio and the estimated copy number of the Dro1 gene in the T1 generation. The result demonstrated that in the T1 generation, the deep rooting ratio of the homozygous plants (copy number of the artificially introduced Dro1 gene: 2) was greater than that of the null type plants (copy number of the artificially introduced Dro1 gene: 0) and heterozygous plants (copy number of the artificially introduced Dro1 gene: 1). Thus, particularly preferred plants of the present invention include transformed plants of the T1 generation where the copy number of the artificially introduced Dro1 gene is 2 (homozygotes), which are produced from transformed plants of the T0 generation where the copy number of the artificially introduced Dro1 gene is 1.

[0220] Specifically, in a particularly preferred embodiment, the present invention include transformed plants produced by methods comprising the steps described below, in addition to the above-described steps (a) to (d) or (a) to (c). In another particularly preferred embodiment, the present invention includes methods for producing transformed plants, which comprise, in addition to the above-described steps (a) to (d) or (a) to (c), the steps of: [0221] producing a plant by crossing the plant transformants obtained in step (d) or (c); and [0222] selecting a plant homozygous for the Dro1 gene from plants obtained in the above step.

[0223] Methods for producing plants of the T1 generation from those of the T0 generation by crossing are known to those skilled in the art. The copy number of the Dro1 gene (null type, heterozygote, and homozygote) in a plant produced by crossing can be determined by methods known to those skilled in the art, such as Southern blot analysis and real-time PCR method.

[0224] Once a transformed plant having a DNA of the present invention introduced into its chromosome is generated, its progeny can be obtained by sexual or asexual reproduction from the plant. Alternatively, the plant can be produced on a large scale from cells, organs, or propagation materials (for example, seeds, fruits, cut panicles, tubers, tuberous roots, stocks, calluses, and protoplasts) isolated from the plants, their progenies, or clones. The present invention includes plant cells artificially introduced with a DNA of the present invention; plants comprising the cells; organs (for example, flower, leaf, root, stem, etc.) of the plants; progenies and clones of the plants; and propagation materials of the plants and their progenies and clones. Such plant cells, plants comprising the cells, organs of the plants, progenies and clones of the plants, and propagation materials of the plants and their progenies and clones can be used to confer a deep rooting trait to plants.

[0225] Meanwhile, transformed plants of the present invention include, for example, monocotyledons. Monocotyledons include, but are not limited to, plants belonging to the Gramineae family, Liliaceae family, Bromeliaceae family, Palmae family, Araceae family, Zingiberaceae family, and Orchidaceae family. Plants belonging to the Gramineae family include, but are not limited to, rice and wheat varieties (wheat, barley, rye, oat, and Job's tears (hatomugi)), corn, millet, foxtail millet, Japanese millet, sorghum, finger millet, pearl millet, teff, sugarcane, timothy, Kentucky bluegrass, orchardgrass, Italian ryegrass, perennial ryegrass, tall fescue, and Bahia grass.

[0226] Furthermore, the present invention relates to processed foods obtained from at least any one of: cells, propagation materials, and organs of the present invention. Herein, processed food refers to a product in an edible form for humans, which is produced by artificially processing plants such as rice, wheat varieties (wheat, barley, rye, oat, and Job's tears (hatomugi)), corn, millet, foxtail millet, Japanese millet, sorghum, finger millet, pearl millet, teff, sugarcane, and timothy, or portions thereof (cells, propagation materials, organs, etc.). In the present invention, processing includes treatments such as boiling, simmering, stir-frying, steaming, frying, and powdering, but is not limited thereto. “Powdering” includes threshing and rice polishing. The processed foods of the present invention include those resulting from at least one of the treatments described above. An example of preferred processed foods of the present invention is: processed foods resulting from threshing and polishing of rice seeds, followed by heating. Specifically, processed foods of the present invention include, but are not limited to, cooked rice products obtained by rice boiling (including frozen cooked rice and sterilized cooked rice), rice powder, rice cake, rice noodle, cubic rice crackers, Japanese rice cracker, cookie, miso (fermented soybean paste), soy sauce, tofu (fermented bean curd), bread, soba (buckwheat noodle), wheat noodle, pasta, noodle such as Chinese noodle (raw noodle, rehydratable noodle, boiled noodle, etc.), cereal, and cornflakes.

[0227] The configuration of processed foods of the present invention as a commercial product is not particularly limited. Examples include the configuration where the product is sold and distributed at an ambient or low temperature and at the time of eating/drinking heated to room temperature or high temperature using a heat cooker such as microwave oven. Specifically, such configuration as a commercial product include, but are not limited to, boxed lunches, rice balls, and cooked noodles, which are sold at convenience stores, supermarkets, delicatessens, and such.

[0228] Processed foods of the present invention may be in a container-packaged form. For example, the foods can be in packaged in a molded plastic container, or packaged in retort pouch or the like and sterilized after sealing.

[0229] “Processed food obtained from at least one of cells, propagation materials, or organs” of the present invention can also be referred to as “processed food produced from at least one of cells, propagation materials, or organs”, “processed food comprising at least one of cells, propagation materials, or organs”, or “processed food obtained by processing at least one of cells, propagation materials, or organs”.

[0230] Furthermore, the present invention provides methods for assessing whether a plant has a deep rooting trait, which comprise steps (a) to (c) described below, wherein a test plant is judged to have a deep rooting trait or to potentially have a deep rooting trait when a molecular weight or nucleotide sequence is identical: [0231] (a) preparing a DNA sample from the test plant; [0232] (b) amplifying from the DNA sample an region comprising the whole or a portion of a DNA of the present invention (Dro1 gene); and [0233] (c) comparing the molecular weight or nucleotide sequence of the amplified DNA fragment with that of the DNA of the present invention (Dro1 gene).

[0234] Such a preferred portion of the Dro1 gene include exon 4 of the Dro1 gene, more preferably regions that comprise a sequence comprising the nucleotide at bp position 116 from the 5′ end of exon 4 of the Dro1 gene (the nucleotide at position 943 in the nucleotide sequence of SEQ ID NO: 2) (for example, regions consisting of at least 100, 50, 40, 30, 20, 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1 nucleotide, which comprise the nucleotide at position 943 in the nucleotide sequence of SEQ ID NO: 2), but is not limited thereto. The present inventors revealed that in Kinandang Patong the nucleotide at bp position 116 from the 5′ end of exon 4 of the Dro1 gene (the nucleotide at position 943 in the nucleotide sequence of SEQ ID NO: 2) is adenine while the nucleotide is deleted in IR64. Thus, whether a test plant has a deep rooting trait can be assessed by examining the presence or absence of this nucleotide. Specifically, the present invention provides methods for assessing whether a plant has a deep rooting trait, which comprise the step of detecting the presence or absence of the nucleotide at position 943 in the nucleotide sequence of SEQ ID NO: 2, wherein a test plant is judged not to have a deep rooting trait when the nucleotide deletion is detected. The single nucleotide deletion can be detected by comparing the nucleotide sequence or molecular weight of a region comprising the whole or a portion of the Dro1 gene.

[0235] Furthermore, the present invention relates to methods for assessing whether a plant has a deep rooting trait, which comprise the step of performing PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 8 and 9, using as a template a genomic DNA prepared from a test plant. In these methods, a test plant is judged to have a deep rooting trait when the amplified product is obtained.

[0236] Furthermore, the present invention relates to methods for assessing whether a plant has a deep rooting trait, which comprise the step of performing PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 10 and 11, using as a template a genomic DNA prepared from a test plant. In these methods, a test plant is judged not to have a deep rooting trait when the amplified product is obtained.

[0237] Furthermore, the present invention provides primers for use in assessing whether a plant has a deep rooting trait. Such primers include, but are not limited to, DNAs comprising the nucleotide sequences of any one of SEQ ID NOs: 8 to 11.

[0238] Herein, “assessing whether a plant has a deep rooting trait” not only means assessing whether a cultivar that has been cultivated so far has a deep rooting trait but also means assessing whether a cultivar newly developed by crossing or using genetic engineering techniques has a deep rooting trait.

[0239] In the methods of the present invention for assessing whether a plant has a deep rooting trait, plants are assessed by testing whether they have a DNA encoding a functional Kinandang Patong-type Dro1 protein. Whether a plant has a DNA encoding a functional (Kinandang Patong-type) Dro1 protein can be assessed by examining genomic DNAs in terms of the difference in the molecular weight or nucleotide sequence of the region corresponding to Dro1.

[0240] In the assessment methods of the present invention, first, a DNA sample is prepared (extracted), and then a DNA region corresponding to the Dro1 gene is amplified from the DNA sample. Next, the molecular weight of the DNA fragment amplified from a DNA region for the Dro1 gene in a cultivar having a deep rooting trait is compared to that of the DNA fragment amplified from a DNA sample of a test plant. The test plant is judged to have a deep rooting trait when the molecular weights are the same. Alternatively, the nucleotide sequence of the DNA fragment amplified from a DNA region for the Dro1 gene in a cultivar having a deep rooting trait is compared to that of the DNA fragment amplified from a DNA sample of a test plant. The test plant is judged to have a deep rooting trait when the nucleotide sequences are identical.

[0241] DNA samples can be prepared (extracted) by methods known to those skilled in the art. Such preferred preparation methods include, for example, methods for extracting DNA by a CTAB method.

[0242] DNA samples to be assessed by the assessment methods of the present invention are not particularly limited. In general, genomic DNAs extracted from test plants are used as DNA samples. Furthermore, sources of genomic DNAs to be collected are not particularly limited, and they may be extracted from any plant tissues, for example, panicles, leaves, roots, stems, seeds, endosperm, bran, or germs. However, the sources are not limited to these examples.

[0243] In the assessment methods of the present invention, a DNA region of the Dro1 gene of the present invention is then amplified by PCR or such. The “DNA region of the Dro1 gene” of the present invention refers to a portion corresponding to the genomic DNA region for the Dro1 gene (for example, the DNA region of SEQ ID NO: 1). The region to be amplified may be the whole genomic DNA or a portion of the genomic DNA (for example, an ORF region encoding the protein or a portion thereof). Those skilled in the art can carry out PCR by appropriately selecting reaction conditions and such. The amplified DNA products can be labeled using primers labeled with isotopes such as .sup.32P, fluorescent dyes, biotin, or such when PCR is carried out. Alternatively, the amplified DNA fragments can be labeled by adding nucleotide substrates labeled with isotopes such as .sup.32P, fluorescent dyes, biotin, or such to PCR mixtures, and carrying out PCR. Furthermore, the amplified DNA fragments can also be labeled after PCR by attaching nucleotide substrates labeled with isotopes such as .sup.32P, fluorescent dyes, biotin, or such, using a Klenow enzyme or the like.

[0244] The labeled DNA fragments obtained in this way are denatured by heating or such, and electrophoresed in a polyacrylamide gel containing a denaturant such as urea or SDS. SDS-PAGE, which uses SDS as a denaturant, is an advantageous fractionation technique in the present invention. SDS-PAGE can be carried out according to the method of Laemmli (Laemmli (1970) Nature 227, 680-685). After electrophoresis, the mobility of the DNA fragments are detected and analyzed by autoradiography using X-ray films, fluorescence-detecting scanners, or such. When labeled DNAs are not used, the DNA fragments can be detected by staining the gel after electrophoresis with ethidium bromide, silver staining, or such. For example, DNA fragments are amplified from a cultivar having a deep rooting trait (for example, Kinandang Patong) and a test plant using primers comprising the nucleotide sequences of SEQ ID NOs: 8 and 9. Whether the test plant has a deep rooting trait can be assessed by comparing their molecular weights. The test plant is judged to have a deep rooting trait when the molecular weights are identical.

[0245] Alternatively, whether a plant has a deep rooting trait can be assessed by directly determining the nucleotide sequence of the DNA region of a test plant corresponding to the DNA of the present invention and comparing the sequence with that of a cultivar having a deep rooting trait. The test plant is judged to have a deep rooting trait when the nucleotide sequences are identical.

[0246] Herein, “identical” means that for both alleles, the molecular weight of the gene or its nucleotide sequence or amino acid sequence is identical to that in a plant having a deep rooting trait. Accordingly, “identical” does not include the case where the molecular weight, nucleotide sequence, or amino acid sequence for one of the alleles is the same as that of a plant having a deep rooting trait but the other is different from that of the plant having a deep rooting trait.

[0247] The above-mentioned electrophoresis analysis may be conducted according to a conventional method. For example, electrophoresis is carried out by applying voltage in an agarose or polyacrylamide gel, and the separated DNA pattern is analyzed.

[0248] Meanwhile, nucleotide sequences can be determined, for example, using DNA sequencers available on the market.

[0249] Furthermore, plants to be identified to have a deep rooting trait can be selected at an early stage by using the assessment methods of the present invention.

[0250] Specifically, the present invention provides methods for selecting a plant having a deep rooting trait, which comprises the steps of (a) and (b) described below: [0251] (a) producing a cultivar by crossing an arbitrary plant with a plant having a deep rooting trait; and [0252] (b) assessing whether a plant produced in step (a) has a deep rooting trait by a method described herein for assessing whether a test plant has a deep rooting trait.

[0253] The selection methods of the present invention may additionally comprise the step of: [0254] (c) selecting a plant that is judged to have a deep rooting trait in step (b).

[0255] A plant having a deep rooting trait can be crossed with an arbitrary plant by methods known to those skilled in the art.

[0256] Plants judged to have a deep rooting trait can be selected at an early stage by using the selection methods of the present invention. The present invention also provides such methods for selecting a plant judged to have a deep rooting trait at an early stage. Herein, “early stage” refers to, for example, the state before heading, preferably the state immediately after germination. By using the selection methods of the present invention, breeding of plant varieties having a deep rooting trait can be achieved in a shorter period of time than ever before.

[0257] Plants to be used in the assessment or selection methods of the present invention include, for example, monocotyledons, but are not limited thereto. Monocotyledons include, but are not limited to, plants belonging to the Gramineae family, Liliaceae family, Bromeliaceae family, Palmae family, Araceae family, Zingiberaceae family, and Orchidaceae family. Plants belonging to the Gramineae family include, but are not limited to, rice, wheat varieties (wheat, barley, rye, oat, and Job's tears (hatomugi)), corn, millet, foxtail millet, Japanese millet, sorghum, finger millet, pearl millet, teff, sugarcane, timothy, Kentucky bluegrass, orchardgrass, Italian ryegrass, perennial ryegrass, tall fescue, and Bahia grass.

[0258] The present invention also provides DNAs (oligonucleotides) comprising at least 15 (for example, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25) consecutive nucleotides complementary to the nucleotide sequence of the Dro1 gene of the present invention or a complementary sequence thereof. Herein, “complementary sequence” refers to the sequence of an opposite strand with respect to the sequence of one strand of a double-stranded DNA consisting of base pairs [A:T] and [G:C]. Furthermore, “complementary” means not only a nucleotide sequence completely complementary to a continuous nucleotide sequence with at least 15 nucleotides but also an identity of at least 70%, preferably at least 80%, more preferably 90%, and still more preferably 95% or more (95%, 96%, 97%, 98%, or 99%) at the nucleotide sequence level. Such DNAs can be used as a probe for detecting or isolating a DNA of the present invention, or as a primer for amplifying the DNA.

[0259] Such primers include, but are not limited to, the primer sets described below: [0260] a primer set consisting of primers comprising the nucleotide sequences of SEQ ID NOs: 4 and 5, which are used to amplify Dro1-INDEL09, an InDel marker for polymorphism between IR64 and Kinandang Patong; [0261] a primer set consisting of primers comprising the nucleotide sequence of SEQ ID NOs: 6 and 7, which are used to amplify Dro1-CAPS05, a CAPS marker for polymorphism between IR64 and Kinandang Patong; [0262] a primer set consisting of primers comprising the nucleotide sequences of SEQ ID NOs: 8 and 9, which are used to amplify SNP02-KP, a Kinandang Patong genomic DNA-specific marker; and [0263] a primer set consisting of primers comprising the nucleotide sequences of SEQ ID NOs: 10 and 11, which are used to amplify SNP02-1R64, an IR64-derived genomic DNA-specific marker.

[0264] Furthermore, the present invention relates to 20 to 100 consecutive nucleotides from the Dro1 gene, which comprise the whole or a portion of a DNA fragment amplified with an above-described primer set using as a template a genomic DNA derived from a plant (for example, rice plant). Such DNAs can be used to assess whether a test plant has the deep or shallow rooting.

[0265] When oligonucleotides of the present invention are used as probes, they are preferably used after appropriate labeling. Labeling methods include, for example, those in which the 5′ end of an oligonucleotide is phosphorylated with .sup.32P using a T4 polynucleotide kinase, and methods in which substrate nucleotides labeled with isotopes such as .sup.32P, fluorescent dyes, biotin, or the like are incorporated into the oligonucleotide by a DNA polymerase such as Klenow enzyme, using as primers random hexamer oligonucleotides or such (random priming methods and the like).

[0266] The oligonucleotides of the present invention can be produced, for example, with a commercially available oligonucleotide synthesizer. The probes can also be produced as double-stranded DNA fragments obtained by restriction enzyme treatment or the like.

[0267] Furthermore, the present invention relates to pharmaceutical agents that confer a deep rooting trait to plants comprising the Dro1 gene or a vector carrying the gene in an expressible manner. The type of DNAs used in the pharmaceutical agents of the present invention is not particularly limited, and the DNAs may be cDNAs or genomic DNAs. In addition, it is possible to use not only DNAs encoding a rice plant-derived Dro1 protein but also DNAs encoding a protein structurally similar to the protein (for example, mutants, derivatives, alleles, variants, and homologs), as long as they can confer a deep rooting trait to a plant when introduced into the plant.

[0268] The DNAs included in the pharmaceutical agents of the present invention may be inserted into vectors. Vectors are not particularly limited, as long as they can allow introduced genes to be expressed in plant cells. For example, it is possible to use vectors containing promoters for homeostatic gene expressions in plant cells (e.g., the promoter of the potato SK2 chitinase gene, the cauliflower mosaic virus 35S promoter, etc.), or vectors containing promoters that are inducibly activated by external stimulation.

[0269] The pharmaceutical agents of the present invention may be DNAs described above or vectors inserted with a DNA described above, and they may be mixed with other ingredients for introduction into plant cells. For example, the DNAs described above, vectors inserted with an above-described DNA, Agrobacteria introduced with an above-described DNA, and biochemical reagents and solutions comprising them are also included in the pharmaceutical agents of the present invention.

[0270] Furthermore, the present invention relates to plants that are transformed with a DNA of the present invention, and which are resistant to drought.

[0271] The present invention also relates to cells, propagation materials, and organs isolated from the plants described above.

[0272] In addition, the present invention relates to processed foods obtained from at least one of cells, propagation materials, and organs described above.

[0273] Moreover, the present invention relates to methods for producing transformed plants resistant to drought, which comprise the steps of introducing a DNA or vector of the present invention into plant cells and regenerating plants from the plant cells.

[0274] The present invention also relates to methods for assessing whether a plant is resistant to drought, which comprise steps (a) to (c) described below, where a test plant is judged to be resistant to drought when a molecular weight or nucleotide sequence is identical. [0275] (a) preparing a DNA sample from a test plant; [0276] (b) amplifying a region comprising a DNA of the present invention from the DNA sample; and [0277] (c) comparing the molecular weight or nucleotide sequence of the DNA of the present invention with that of the amplified DNA fragment.

[0278] The present invention also relates to methods for assessing whether a plant is resistant to drought, which comprise the step of carrying out PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 8 and 9 using as a template a genomic DNA prepared from a test plant, wherein the test plant is judged to be resistant to drought when PCR yields an amplification product.

[0279] Furthermore, the present invention relates to methods for assessing whether a plant is resistant to drought, which comprise the step of carrying out PCR with primers comprising the nucleotide sequences of SEQ ID NO: 10 and 11 using as a template a genomic DNA prepared from a test plant, wherein the test plant is judged not to be resistant to drought when PCR yields an amplification product.

[0280] In addition, the present invention relates to methods for selecting drought-resistant plants, which comprise the steps of: [0281] (a) producing a cultivar by crossing an arbitrary plant with a drought-resistant plant; and [0282] (b) assessing whether a plant produced in step (a) is resistant to drought by the above-described method for assessing whether a plant is resistant to drought.

[0283] The production of transformed plants that are resistant to drought, assessment of plants for drought resistance, and selection of drought-resistant plants can be achieved according to the description herein.

[0284] Whether a plant is resistant to drought can be assessed by measuring the leaf temperature.

[0285] Herein, as long as the leaf temperature of a plant transformant is decreased under an artificial drought stress condition (under a dry environment) as compared to a control, even if the temperature drop is very small, the plant is judged to “be resistant to drought”.

[0286] Herein, leaf temperature refers to the leaf surface temperature of a plant. Plants absorb carbon dioxide through stomata for photosynthesis. At the same time, the intracellular water evaporates through stomata into the atmosphere. This results in a loss of water. The phenomenon is called transpiration. With regard to these connections, Takai et al., have reported that the leaf temperature has a negative correlation to the photosynthesis rate and degree of stoma dilation (stomatal conductance) (Takai et al., Field Crops Research doi:10.1016/j.fcr.2009.10.019. 2009). The more stomata open, the more active the transpiration becomes. Transpiration takes heat away from the leaf surface, resulting in a reduction of the leaf temperature. When a plant is actively photosynthesizing, it opens stomata, and transpiration becomes active. This results in a temperature decrease at the leaf surface. Meanwhile, under drought stress, the plant suppresses transpiration by closing stomata to maintain the cellular water potential. This impairs photosynthesis and raises the leaf surface temperature. Drought-resistant plants, which can open the stomata and photosynthesize even under drought conditions, have a lower leaf temperature as compared to drought-sensitive plants. Hirayama et al. have reported that selection of drought-resistant rice plant lines using the leaf temperature as an indicator is effective in developing drought-resistant rice cultivars (Hirayama et al., Breeding Science 56: 47-54. 2006). As described in the Examples herein, whether a plant has a low leaf temperature can be assessed simply by testing it under drought stress using a device such as infrared thermography. Meanwhile, the photosynthesis and degree of stoma dilation can be assessed by simple tests under drought stress using a device such as the photosynthesis/transpiration measurement system, as described in the Examples herein.

[0287] Furthermore, it is known that in general plants exhibit leaf curling when exposed to drought stress. In particular, rice plant leaves are known to roll into a needle-like shape. However, the transformed plants of the present invention hardly show leaf curling even under drought stress.

[0288] Specifically, the present invention relates to plants that are transformed with a DNA of the present invention, and which are resistant to leaf curling under drought stress.

[0289] The present invention also relates to cells, propagation materials, and organs isolated from the plants described above.

[0290] The present invention also relates to processed foods obtained from at least one of the cells, propagation materials, and organs described above.

[0291] Furthermore, the present invention relates to methods for producing transformed plants resistant to leaf curling under drought stress, which comprise the steps of introducing a DNA or vector of the present invention into plant cells and regenerating plants from the plant cells.

[0292] The present invention also relates to methods for assessing whether a plant is resistant to leaf curling under drought stress, which comprise steps (a) to (c) described below, where a test plant is judged to be resistant to leaf curling under drought stress when a molecular weight or nucleotide sequence is identical: [0293] (a) preparing a DNA sample from a test plant; [0294] (b) amplifying a region comprising a DNA of the present invention from the DNA sample; and [0295] (c) comparing the molecular weight or nucleotide sequence of the DNA of the present invention with that of the amplified DNA fragment.

[0296] The present invention also relates to methods for assessing whether a plant is resistant to leaf curling under drought stress, which comprise the step of carrying out PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 8 and 9 using as a template a genomic DNA prepared from a test plant, wherein the test plant is judged to be resistant to leaf curling under drought stress when PCR yields an amplification product.

[0297] Furthermore, the present invention relates to methods for assessing whether a plant is resistant to leaf curling under drought stress, which comprise the step of carrying out PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 10 and 11 using as a template a genomic DNA prepared from a test plant, wherein the test plant is judged not to be resistant to leaf curling under drought stress when PCR yields an amplification product.

[0298] In addition, the present invention relates to methods for selecting plants that are resistant to leaf curling under drought stress, which comprise the steps of: [0299] (a) producing a cultivar by crossing an arbitrary plant with a plant that is resistant to leaf curling under drought stress; and [0300] (b) assessing whether a plant produced in step (a) is resistant to leaf curling under drought stress by the above-described method for assessing whether a plant is resistant to leaf curling under drought stress.

[0301] The production of transformed plants that are resistant to leaf curling under drought stress, assessment of whether a plant is resistant to leaf curling under drought stress, and selection of plants that are resistant to leaf curling under drought stress can be achieved according the description herein.

[0302] Herein, leaf curling resistance refers to resistance to the leaf curling caused by drought stress. When rice plant leaves become dehydrated, the turgor pressure of epicuticular motor cells is reduced inside the leaves and as a result they curl so that the epicuticular side becomes concave. Whether a plant is resistant to leaf curling can be assessed simply by testing whether its leaves curl under drought stress.

[0303] Herein, as long as the degree of leaf curling in a plant transformant is smaller when compared to a control, even if the difference in the degree is very slight, the plant is judged to “be resistant to leaf curling”.

[0304] Furthermore, under drought stress conditions, crop plants are in general often severely infertile, resulting in a decrease in the number of ripened grains and ripened grain weight. This leads to a reduction in the ultimate crop yield. However, even under drought stress, the transformed plants of the present invention produce a greater number of ripened grains or heavier ripened grains (reduction in the number of ripened grains or ripened grain weight has been suppressed) as compared to plants without having a DNA of the present invention (control).

[0305] Specifically, the present invention relates to plants transformed with a DNA of the present invention, which produce a greater number of ripened grains or heavier ripened grains as compared to a control under drought stress. Such a plant can also be referred to as a plant that has been improved to reduce a loss in the number of ripened grains or ripened grain weight under drought stress. Alternatively, the plant can be referred to as a plant that has been improved to have an increased number of ripened grains or increased ripened grain weight under drought stress as compared to a control.

[0306] Furthermore, the present invention relates to cells, propagation materials, and organs isolated from the plants described above.

[0307] The preset invention also relates to processed foods produced from at least one of the cells, propagation materials, and organs described above.

[0308] Moreover, the present invention relates to methods for producing a transformed plant that produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control, which comprise the steps of introducing a DNA or vector of the present invention into plant cells and regenerating plants from the plant cells.

[0309] In addition, the present invention relates to methods for assessing whether a plant produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control, which comprise steps (a) to (c) below, wherein a test plant is judged to produce a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control when a molecular weight or nucleotide sequence is identical: [0310] (a) preparing a DNA sample from a test plant; [0311] (b) amplifying a region comprising a DNA of the present invention from the DNA sample; and [0312] (c) comparing the molecular weight or nucleotide sequence of the DNA of the present invention with that of the amplified DNA fragment.

[0313] The present invention also relates to methods for assessing whether a plant produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control, which comprise the step of carrying out PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 8 and 9 using as a template a genomic DNA prepared from a test plant, wherein the test plant is judged to produce a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control when PCR yields an amplification product.

[0314] Furthermore, the present invention relates to methods for assessing whether a plant produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control, which comprise the step of carrying out PCR with primers comprising the nucleotide sequences of SEQ ID NOs: 10 and 11 using as a template a genomic DNA prepared from a test plant, wherein the test plant is judged not to produce a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control when PCR yields an amplification product.

[0315] In addition, the present invention relates to methods for selecting plants that produce a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control, which comprise the steps of: [0316] (a) producing a cultivar by crossing an arbitrary plant with a plant that produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control; and [0317] (b) assessing whether a plant created in step (a) produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control by the above-described method for assessing whether a plant produces a greater number of ripened grains or heavier ripened grains under drought stress as compared to a control.

[0318] The production, assessment, and selection of the plants described above can be achieved according to the description herein.

[0319] Herein, “produce a greater number of ripened grains or heavier ripened grains” means that the number of grains ripened under drought stress is greater or the weight of grain ripened under drought stress is heavier when compared to a control without having a DNA of the present invention. Herein, as long as the number of ripened grains is greater or the ripened grain weight is heavier when compared to the control, even if the difference is very small, the plant is judged to “produce a greater number of ripened grains or heavier ripened grains”.

[0320] The number of ripened grains of a plant can be readily determined, for example, by counting ripened grains in harvested panicles excluding infertile panicles. However, the determination method is not limited to this example. Meanwhile, the ripened grain weight of a plant can be readily determined, for example, by weighing ripened grains in harvested panicles excluding infertile panicles. However, the determination method is not limited to this example.

[0321] SEQ ID NOs corresponding to respective sequences are listed below: [0322] SEQ ID NO: 1, the genomic DNA nucleotide sequence for the Dro1 gene of Kinandang Patong; [0323] SEQ ID NO: 2, the cDNA nucleotide sequence for the Dro1 gene of Kinandang Patong; [0324] SEQ ID NO: 3, the amino acid sequence of the Dro1 protein of Kinandang Patong; [0325] SEQ ID NOs: 4 and 5, a primer set used for amplifying Dro1-INDEL09, an InDel marker for polymorphism between IR64 and Kinandang Patong; [0326] SEQ ID NOs: 6 and 7, a primer set used for amplifying Dro1-CAPS05, a CAPS marker for polymorphism between IR64 and Kinandang Patong; [0327] SEQ ID NOs: 8 and 9, a primer set used for amplifying SNP02-KP, a Kinandang Patong genomic DNA-specific marker; [0328] SEQ ID NOs: 10 and 11, a primer set used for amplifying SNP02-IR64, an IR64 genomic DNA-specific marker [0329] SEQ ID NO: 12, the CDS nucleotide sequence of the sorghum Dro1 gene; [0330] SEQ ID NO: 13, the amino acid sequence of the sorghum Dro1 protein; [0331] SEQ ID NO: 14, the CDS nucleotide sequence of the corn Dro1 gene; [0332] SEQ ID NO: 15, the amino acid sequence of the corn Dro1 protein; [0333] SEQ ID NO: 16, the cDNA nucleotide sequence of Nipponbare used in the FOX hunting system [This sequence has a 1-bp addition at each of the 5′ and 3′ ends when compared to the cDNA sequence (the nucleotide sequence of SEQ ID NO: 2) determined based on the genomic DNA nucleotide sequence. Furthermore, this cDNA had a nucleotide substitution of G for A at bp position 373 from the 5′ end in its nucleotide sequence (at bp position 372 from the 5′ end in SEQ ID NO: 2).]; [0334] SEQ ID NO: 17, the nucleotide sequence of the Dro1 gene of Kinandang Patong and its upstream sequence including the promoter region; and [0335] SEQ ID NO: 18, the nucleotide sequence of a region in Nipponbare that corresponds to SEQ ID NO: 17.

[0336] All prior art documents cited herein are incorporated herein by reference.

EXAMPLES

[0337] In the present invention, a basket method was improved to enable simple, reproducible assessment of deep rooting in a space-saving way. Furthermore, a callus-based Agrobacterium transformation method was improved to introduce candidate nucleotide sequences into IR64, and the gene was introduced into IR64. The nucleotide sequence of Dro1, which is the deep rooting gene, was isolated and identified by a map-based cloning method. Thus, the present inventors developed techniques for conferring drought avoidance ability to rice plants by easily modifying the deep rooting using the gene.

[0338] Hereinbelow, the present invention will be specifically described with reference to the Examples, but it is not to be construed as being limited thereto.

Example 1

Identification of Dro1 Gene Locus

[0339] Two rice cultivars: Kinandang Patong (a Philipino upland rice variety) and IR64 (a paddy-field rice cultivar developed by the International Rice Research Institute) were distributed by the International Rice Research Institute. The two cultivars were crossed with each other to obtain materials for gene isolation. Among the BC.sub.2F.sub.2 population which results from crossing of the two cultivars, a population segregated at chromosome 9 but fixed to IR64 homozygous as much as possible in the other chromosomal regions segregated into shallow-rooted plants and deep-rooted plants. IR64 and Kinandang Patong show the shallow rooting type and deep rooting type, respectively. Therefore, the gene responsible for deep rooting of Kinandang Patong was assumed to be involved in the segregation. From the perspective described above, the inventors thoroughly evaluated the population and divided the plants into shallow rooting and deep rooting types to investigate the genotypes. The result showed that the quantitative trait locus (QTL) related to the deep rooting was located on chromosome 9 (Uga et al., The 2nd International Conference on Plant Molecular Breeding. 2007). A detailed genetic analysis was carried out by using the basket method that enables quantitative assessment of the deep rooting. Specifically, plastic baskets with a diameter of 15 cm were filled with soil and buried in pots. After sowing, rice plants were cultivated until they reached about leaf age 8. The deep rooting was assessed based on the deep rooting ratio, which was defined as the percentage of roots penetrating the bottom of the basket with respect to the total number of roots penetrating each basket. The baskets have flat bottoms. When extending downward more than 53° with respect to ground surface, the root penetrates the basket bottom. The mean deep rooting ratio was 1.6% for IR64, whereas the mean ratio of Kinandang Patong was 72.6%. To map the QTL related to the deep rooting as a single locus, eight plants having recombinations in a region near the QTL were selected from BC.sub.2F.sub.2 population. Then, inbred fixed lines (BC.sub.2F.sub.4) were selected from the selfed progenies (BC.sub.2F.sub.3). From each fixed line, 20 to 23 plants were cultivated in a pot. The genotypes were deduced from the deep rooting ratio determined by the basket method. From the BC.sub.2F.sub.4 line, strains whose region around QTL were fixed in the IR64 type showed a mean deep rooting ratio of 2.6%, which was almost comparable to that of IR64. Meanwhile, stains whose regions around QTL were fixed in the Kinandang Patong type exhibited a mean deep rooting ratio of 40.4%. Their QTL genotypes were clearly determined from these results. The QTL was mapped as a single locus located between InDel markers: ID07_14 and ID07_17. Thus, the QTL was named deep rooting-related locus “Dro1” (Deeper Rooting 1) (Uga et al., Nihon Ikusyu Gakkai Dai 112 Kai Kouenkai Youshisyu (112nd Meeting of The Japanese Society of Breeding, Program and Abstracts) PP. 188, 2007; Uga et al., Dai 27 Kai Ne Kenkyu Syukai (27th Research Meeting of The Japanese Society for Root Research), 2007; Uga et al., The 5th International Crop Science Congress Abstracts 243p. 2008). Furthermore, all SSR markers located in the region between the two InDel markers were assessed by polymorphism analysis based on public information on simple sequence repeat (SSR) markers (International Rice Genome Sequencing Project 2005). The candidate region for Dro1 was narrowed down to 608 kbp located between SSR markers: RM24393 and RM7424.

Example 2

High-Resolution Linkage Analysis

[0340] To isolate the Dro1 gene by a map-based cloning method, 359 plants having recombinations within the candidate region were selected from BC.sub.3F.sub.2 population consisting of 4,560 plants. A large number of plants had to be assessed at one time for their deep rooting ratio to narrow down the candidate region using progenies of the selected plants. Then, the present inventors developed an evaluation method that enables hydroponical cultivation without burying baskets in pots. In the improved basket method developed by the present inventors, custom-made stainless-steel baskets with a diameter of 7.5 cm filled with soil were placed in a hydroponic medium, instead of being buried in pots. Thus, the method enables one to assess rice plants for the deep rooting ratio in one fourth of the space required in the original method. In the improved basket method, the deep root was defined as extending downward more than 50° with respect to ground surface (FIG. 1). Using the improved basket method, the deep rooting ratio was determined by assessing about 40 plants per line. The genotype of Dro1 gene in each line was predicted based on the frequency distribution of the deep rooting ratio. To narrow down the gene region, DNA markers were selected by screening. The information about SNPs located near the Dro1 in Azucena, a cultivar closely related to IR64 and Kinandang Patong, was extracted from the homepage of OryzaSNP Consortium (http://irfgc.irri.org/index.php?option=com_content&task=view&id=14&Itemid=106) for the designing of CAPS markers. The CAPS markers were tested for polymorphisms. As a result, six markers detected polymorphisms between IR64 and Kinandang Patong, and the six polymorphism markers were used in mapping. Furthermore, BAC libraries of IR64 and Kinandang Patong were constructed, and screened for clones comprising the candidate region. The selected clones were analyzed by nucleotide sequencing. The resulting sequence information was used to prepare 11 types of InDel markers and CAPS markers for polymorphism between IR64 and Kinandang Patong. Recombinant lines were selected from 359 lines using these markers. By linkage analysis, the Dro1 gene region was narrowed down to a 6.0-kbp region between an In Del marker Dro1-INDEL09 (primers: 5′-GCAGACGCTCGTAACACGTA-3′ (SEQ ID NO: 4) and 5′-GTGGCAGCTCCATCAACTCT-3′ (SEQ ID NO: 5)) and a CAPS marker Dro1-CAPS05 (primers: 5′-GCACAAGATGGGAGGAGAGT-3′ (SEQ ID NO: 6) and 5′-CATGGGTGAGAATCGTGTTG-3′ (SEQ ID NO: 7); the amplified DNA is digested with restriction enzyme Hinf I). A RAP-DB analysis of the genomic nucleotide sequence comprising the candidate region revealed the presence of one predicted gene. The predicted gene was found to have 1-bp deletion in exon 4 of the IR64 sequence that causes a frame shift, resulting in a stop codon.

Example 3

Complementation Test for Identifying the Dro1 Gene and Assessment of the Deep Rooting Ratio in Dro1 Gene-Overexpressing Plants

3.1 Complementation Test for Identifying the Dro1 Gene

[0341] The gene predicted by RAP-DB was presumed to be Dro1. A Kinandang Patong-derived 8.7-kbp KpnI-NotI fragment covering the 6.0-kbp candidate region for Dro1 and their upstream and downstream regions was inserted into pPZP2H-lac (Fuse et al., Plant Biotechnology 18: 219-222, 2001), and introduced into calluses of IR64 through Agrobacterium EHA101. Specifically, transformation of IR64 was carried out as follows.

(Induction of Calluses for Agrobacterium Infection)

[0342] Sterilized IR64 seeds were placed in a callus induction medium containing 2,4-D, and cultured at 30 to 33° C. for one week under continuous light. Then, the calluses were divided and transferred into a fresh callus induction medium. This procedure was repeated three times for callus formation. The callus induction medium used was modified from NBPRCH40 (Hiei and Komari Nature Protocols 3: 824-834. 2008), which had been used in Hiei and Komari for preculturing calluses for redifferentiation of plant transformants after selection of calluses transformed by the immature embryo method. The callus induction medium has the following composition:

[0343] 100 mL of 10× N6 major salts, 10 mL of 100× Fe-EDTA, 1 mL of 1,000× B5 minor salts, 1 mL of 1,000× B5 vitamins, 30 g/L maltose, 0.5 g/L casamino acids, 0.5 g/L proline, 2 mg/L 2,4-D, and 5 g/L Gelrite (pH 5.8).

(Agrobacterium Infection)

[0344] Prior to infection, calluses are transferred into a fresh medium. After three days of preculture, the calluses were soaked in an Agrobacterium suspension. Then, the calluses were transferred into 2N6-AS medium (Hiei and Komari, Nature Protocols 3: 824-834. 2008) and co-cultured at 23° C. in the dark.

(Removal of Bacteria and Selection of Transformed Calluses)

[0345] Agrobacterium was removed after co-culture. Then, in order to select transformed cells, the transformed calluses were placed in a callus induction (selection) medium containing drugs (25 mg/L Hygromycin and 400 mg/L carbenicillin). After one week of culture at 30 to 33° C. under continuous light, the calluses were divided and transferred into a fresh selection medium. This procedure was repeated three times to select the transformed cells.

(Redifferentiation from Transformants)

[0346] The calluses grown in the selection medium were transferred into a redifferentiation medium. After one week to 10 days of culture at 28° C. under continuous light, sprouting calluses were transferred into a fresh redifferentiation medium. This procedure was repeated twice to select transformed plants. The composition of the redifferentiation medium is as follows: 100 mL of 10× N6 major salts, 10 mL of 100× Fe-EDTA, 1 mL of 1,000× B5 minor salts, 1 mL of 1,000× B5 vitamins, 30 g/L maltose, 30 g/L sorbitol, 2g/L casamino acids, 0.5 g/L proline, 0.02 mg/L NAA, 5 g/L, 2 mg/L kinetin, and 5 g/L Gelrite (pH 5.8). Hygromycin and carbenicillin were added at 25 mg/L and 300 mg/L to the prepared medium, respectively.

(Naturalization)

[0347] The redifferentiated transformants were transferred and cultured in a rooting medium (MS medium (4 g/L Gelrite (pH 5.8) supplemented with 25 mg/L Hygromycin and 200 mg/L carbenicillin)) at 28° C. under continuous light. The transformed plants were naturalized after confirmation of root growth.

[0348] The 17 independent callus-derived transformant clones obtained through Hygromycin selection were tested for their deep rooting ratio in the first generation (T0) by the improved basket method. Among lines introduced with the Kinandang Patong-derived 8.7-kbp fragment a number of lines showed a high deep rooting ratio, whereas the deep rooting ratio in the vector control was the same as that of IR64 (FIGS. 1 and 2). The copy number of the transformation vector introduced into each plant of the T0 generation was determined by the combined use of Southern analysis and a real-time PCR system that allows detection of the sequence of the Hygromycin-resistant gene in the transformation vector. Plants carrying the gene in a single copy were selected and T1 seeds were produced. The null type (0 copy), heterozygote (1 copy), and homozygote (2 copies) of T1 plants from four lines with single-copy T0 were inferred based on the signal intensities obtained by the real-time PCR system, and the correlation with the deep rooting ratio was evaluated. In all of the four lines, plants with zero signal intensity showed the same deep rooting ratio as plants with the control vector (FIG. 3). Meanwhile, lines with a strong intensity exhibited a high deep rooting ratio. For example, two lines of D27-c were speculated to be a null type, because their signal intensities were zero and their deep rooting ratios were low. Meanwhile, four lines with a signal intensity of about 10 to 20 showed a medium deep rooting ratio and thus were assumed to be the heterozygous type; and all four lines with a signal intensity of about 40 to 70 exhibited a high deep rooting ratio, and therefore were judged to be the homozygous type. As described above, in T1 lines with a single copy of Dro1, a positive correlation was found between the deep rooting ratio and the genotype segregation for the introduced Dro1 gene.

3.2 Assessment of Dro1 Gene-Overexpressing Plants for Their Deep Rooting Ratio

[0349] A full-length cDNA (AK068870) for the putative gene has been registered in RAP-DB. Two Nipponbare lines for each of the T1 and T2 generations are available on the FOX hunting system (Full-length cDNA Over-eXpressing gene hunting system). The full-length cDNA sequence (SEQ ID NO: 16) used for the FOX lines has a 1-bp addition at each of the 5′ and 3′ ends when compared to the cDNA sequence (SEQ ID NO: 2) determined from the genomic nucleotide sequence. Furthermore, this cDNA had a nucleotide substitution of G for A at bp position 373 from the 5′ end in its nucleotide sequence (at bp position 372 from the 5′ end in SEQ ID NO: 2). The nucleotide substitution resulted in a non-synonymous amino acid substitution of glutamic acid for lysine at position 37 in SEQ ID NO: 3. Five plants from each of the four lines were assessed for their deep rooting ratio by the improved basket method. The result showed that in the FOX lines the deep rooting ratio ranged from 8.1 to 50.0% while the ratio was between 12.2 and 23.5% for ten wild type Nipponbare (control). Thus, plants of the FOX lines include those exhibiting a deep rooting ratio significantly higher than Nipponbare (FIG. 4).

[0350] The result demonstrated that the predicted gene in the 6.0-kbp candidate region was the true Dro1. Meanwhile, the complementation test result suggested that the Kinandang Patong-type Dro1 was the functional form responsible for deep rooting, while the IR64-type Dro1 had lost the function or its function was impaired, resulting in shallow rooting.

[0351] Two lines (T1) having Dro1 in multicopies were assessed for the relation between signal intensity and deep rooting ratio. In D130-c, a positive correlation was found between signal intensity and deep rooting ratio (FIG. 3). Meanwhile, with respect to D91-e, a positive correlation was observed between signal intensity and deep rooting ratio in four plants that gave a signal intensity comparable to that of the homozygote with a single copy of the gene (10 to 350); however, six lines with a high signal intensity (500 to 2,000) had the same shallow rooting as that of the vector control. Introduction of Dro1 in multicopies was assumed to cause gene silencing in the plants. This suggests that it is necessary to adjust the expression level of the Dro1 gene, for example, by selecting plants having a single copy of the gene at the time of introduction.

Example 4

Amino Acid Sequence Homology Among Rice, Sorghum, and Corn Dro1

[0352] Using the amino acid sequence of Dro1 as a query, genes homologous to Dro1 were searched by blastn on the NCBI homepage (http://blast.ncbi.nlm.nih.gov/Blast.cgi). The search identified highly homologues genes; one was a sorghum gene, and the other was a corn gene. In both sorghum and corn, the ORF with the highest homology to Dro1 had no gene name. Thus, the present inventors named the sorghum and corn genes “SbDro1L1” and “ZmDro1L1”, respectively. The amino acid sequence for the sorghum gene was available on the NCBI homepage. Meanwhile, the amino acid sequence for the corn gene was obtained from MaizeGDB (http://www.maizegdb.org/) via search based on the mRNA sequence extracted at NCBI. The nucleotide sequence of SbDro1L1 CDS is shown in SEQ ID NO: 12, and the amino acid sequence is shown in SEQ ID NO: 13. On the other hand, the nucleotide sequence of ZmDro1L1 CDS is shown in SEQ ID NO: 14, and the amino acid sequence is shown in SEQ ID NO: 15. SbDro1L1 and ZmDro1L1 showed 64% and 62% homology to Dro1, respectively (FIG. 5).

Example 5

Effect of Dro1 on the Deep Rooting Under Field Condition

[0353] The present inventors assessed whether Dro1 was responsible for deep rooting under field conditions. The near-isogenic lines (Dro1-NIL) used as an experimental material in the field test were developed by the following method. IR64/Kinandang Patong F.sub.1 was backcrossed with IR64 four times, followed by a selfing. From the resulting BC.sub.4F.sub.2 lines, plants homozygous only for the 16.6- to 19.5-Mbp region on chromosome 9 were selected, and selfed seeds from the lines were used as the near-isogenic lines. Seeds of IR64, Kinandang Patong, and Dro1-NIL were planted in an upland field and grown under fertilization management commonly used for upland rice plants. The plants were grown for 105 days under rainfed conditions. The soil near the plant was removed to a depth of about 1 m with a loading shovel. Then, the exposed surface was washed thoroughly with water spray up to about 5 cm from the plant in order to observe maximum root depth. The result showed that the root depth of IR64, Kinandang Patong, and Dro1-NIL in soil was about 20, 80, and 40 cm, respectively (FIG. 6). The root length of Dro1-NIL was the same as that of IR64. However, the root growth depth of Dro1-NIL was about twice as that of IR64. Thus, the root growth angle was increased due to the effect of Dro1, and as a result the roots of Dro1-NIL extended deeper up to the same depth (about 40 cm) as the root length of IR64.

Example 6

Effect of Dro1 on Drought Resistance in the Experimental Field for Testing Drought Resistance

[0354] The present inventors tested whether the deep rooting due to Dro1 improved drought resistance. IR64 and Dro1-NIL were used as experimental material in the drought resistance test. The same drought resistance test facility used in the Plant Biotechnology Institute, Ibaraki Agricultural Center (Hirayama and Suga, Nougyo Kenkyu Senta Kenkyu Shiryo Dai 30 Gou, Ine Ikusyu Manyuaru (Agricultural Research Center Research Data NO. 30; Rice plant breeding manual) 152-155. 1995) was arranged in a plastic greenhouse at the inventors' Institute to carry out the drought resistance test. The facility includes an irrigation area and a drought stress area. In the irrigation area, 30 cm of additional topsoil within a wooden frame was placed on the floor soil. In the irrigation area, rice plants were watered intermittently to avoid drought stress during the period between sowing and harvesting. During the cultivation period, the soil water potential was monitored by a tensiometer placed in soil at a depth of 25 cm, and irrigation was applied when the potential was below about −0.015 MPa (FIG. 7). In general, plants do not suffer from drought stress at this level. Meanwhile, in the drought stress area, 10-mm gravel (5 cm thick) was layered on the bed soil of the experimental field and 25 cm additional topsoil was placed on it to block capillary water from the soil. Under this arrangement, the soil water content in the additional topsoil layer is gradually reduced and the plants are exposed to drought stress when irrigation is terminated. In the drought stress area, irrigation was terminated about two months after sowing and the plants were not watered until the first panicle appearance. The soil water potential at a depth of 25 cm was reduced to −0.07 MPa 10 days after irrigation was terminated. As a result, the drought stress condition was achieved in the drought stress area (FIG. 7). On the other hand, at 40 cm soil depth, the water potential was stable at about −0.03 MPa throughout the period of stress treatment. Thus, the drought stress condition was not achieved at this depth. In the drought stress area, leaf rolling was observed in IR64 on day 35 after the termination of irrigation, suggesting the drought stress effect. In contrast, leaf rolling was not detected in IR64 having Kinandang Patong-type Dro1 (Dro1-NIL) (FIG. 8). Then, the degree of leaf rolling in IR64 was increased in the stress area, and on day 49 the growth of the plants was revealed to be severely suppressed. Meanwhile, in Dro1-NIL, the degree of leaf rolling remained low even on day 49, and the plant growth was vigorous when compared to IR64. The mean leaf temperature of Dro1-NIL was 0.7° C. lower than that of IR64 on day 35 after the termination of irrigation in the drought stress area (FIG. 9). The leaf temperature of Dro1-NIL was revealed to be lower than that of IR64 on every measurement day. Furthermore, twice on days 34 and 41, IR64 and Dro1-NIL were also measured for the stomatal conductance and photosynthesis rate. The result showed that both values of Dro1-NIL were significantly greater than those of IR64 (FIG. 9). After the first panicle appearance in the drought stress area, the plants were watered again for rice grain ripening. Each plant was separately harvested, and assessed for their culm length, panicle length, panicle number, panicle weight, number of filled grains, and the dry matter weight of their aerial part. No significant difference was observed in the culm and panicle lengths between IR64 and Dro1-NIL. Meanwhile, the dry matter weight of their aerial part, panicle number, panicle weight, and number of filled grains were significantly different between IR64 and Dro1-NIL (FIG. 10). In particular, the number of filled grains in Dro1-NIL was about 3.8 times greater than that of IR64. To ascertain whether the deep rooting of Dro1-NIL was responsible for this result, the experimental field was dissected to observe whether the roots penetrated the gravel layer. The result revealed that the roots of Dro1-NIL penetrated through the gravel layer into the deeper soil layer whereas the roots of IR64 could not penetrate through the gravel layer (FIG. 11). The findings described above demonstrated that rice plants acquired drought resistance from the deep rooting conferred by Dro1, resulting in increases in the photosynthesis ability and yield.

[0355] Meanwhile, the leaf temperature was measured using a device for displaying temperature distribution images by detecting the energy of infrared emitted from the subject and converting it into an apparent temperature (infrared thermography). Specifically, the leaf surface temperature of rice plants under a drought stress condition was measured by infrared thermography from a fixed distance. Then, the images were exported with exclusive software to determine the mean leaf temperatures of plants on the images. The photosynthesis rate was estimated by placing leaves in a chamber aerated with air containing a constant concentration of carbon dioxide and measuring the decrease of carbon dioxide concentration in the chamber output air. Meanwhile, the stomatal conductance was estimated by measuring the increase of water vapor content in the output air from the chamber containing the leaf. Specifically, the values were determined as follows. Fully expanded leaves from rice plants under a drought stress condition were each held nipped for a fixed period of time in the chamber of the photosynthesis transpiration measurement system. The same expanded leaves were measured in triplicate to determine the mean value.

Example 7

Drought Resistant Effect of Dro1 in an Upland Field Under Severe Drought

[0356] In Example 6, Dro1 was demonstrated to be responsible for drought resistance in the experimental field for testing drought resistance. Then, the present inventors assessed whether Dro1 results in drought resistance even under greater drought stress in the natural environment of a crop field. Experiment was carried out using IR64 and Dro1-NIL in an upland field in triplicate for areas with (N:P:K=12:12:9 kg/10 a) and without fertilizer. In each area (3 m×3 m), 200 plants were planted with a spacing of 30 cm between rows and 15 cm between plants. The 200 plants consisted of 100 plants each of IR64 and Dro1-NIL. The plants were not watered during cultivation. Thus, the drought stress condition was severe, and the mean soil water potential was −0.08 MPa below at 40 cm soil depth (FIG. 12), because there was no rainfall for one month from 90 days after sowing. Under the drought stress condition, leaf rolling was hardly detectable in Dro1-NIL while severe leaf rolling was observed for IR64 in both areas (FIG. 13). Particularly, in the area without fertilizer, leaf rolling was hardly detected in Dro1-NIL, whereas IR64 showed leaf rolling and the heading date was significantly delayed as compared to that of Dro1-NIL. The yields were estimated by the quadrate method in the harvest season. Of the five parameters investigated, four parameters namely, panicle number, dry matter weight of aerial part, total grain weight, and filled grain weight, had greater values in Dro1-NIL than in IR64 (Table 1).

TABLE-US-00001 TABLE 1 YIELD TRAITS OF RICE PLANTS GROWN IN AN UPLAND FIELD UNDER SEVERE DROUGHT DRY MATTER DRY MATTER WEIGHT OF WEIGHT OF TOTAL GRAIN FILLED GRAIN PANICLE AERIAL PART STEM LEAF WEIGHT WEIGHT NUMBER (g) (g) (g) (g) TREATMENT LINE Mean S.D. Mean S.D. Mean S.D. Mean S.D. Mean S.D. NON- IR64 347.3 ±  5.0 a 1391.5 ± 124.1 a 1288.6 ± 112.6 a 102.9 ± 13.3 a    21.9 ± 21.8 a FERTILIZA- Dro1-NIL 394.3 ± 12.2 bc 1511.7 ±  36.4 b 1256.1 ±  79.5 b 255.6 ± 60.4 b  107.3 ± 50.6 ab TION Dro1-NIL/IR64(%) 113.5  108.6  97.5 248.4 [00001] FERTILIZA- IR64 419.3 ± 39.4 ab 1710.7 ± 194.2 ab 1612.3 ± 198.3 a  98.4 ±  9.5 a    8.9 ±  7.9 a TION Dro1-NIL 457.0 ± 28.2 c 1733.8 ± 106.6 b 1541.9 ± 118.1 b 192.0 ± 54.5 b   69.9 ± 48.0 b Dro1-NIL/IR64(%) 109.0  101.4  95.6 195.0 [00002] Mean: MEAN VALUE FOR A TOTAL OF 24 PLANTS PER AREA IN TRIPLICATE, S.D.: STANDARD DEVIATION THE DIFFERENT ALPHABETICAL LETTERS INDICATE A SIGNIFICANT DIFFERENCE OF 5% IN A PAIRWISE COMPARISON BY Student's t-TEST.

[0357] In particular, the filled grain weight, which is the major factor for the yield, was greatly increased to 4.9 times in the area without fertilizer and to 7.8 times in the area with fertilizer.

[0358] This finding demonstrates that Dro1 resulted in drought resistance in the natural cultivation environment of a crop field even under drought conditions.

Example 8

Markers for Examining the Presence of Single Nucleotide Deletion in the Dro1 Gene

[0359] Since the Dro1 gene sequence of IR64 has a 1 base deletion in its exon 4, PCR markers were designed to test the presence of the deletion. The two types of designed markers were: SNP02-KP (primers: 5′-GTCTAGATCACGCAGTGAAT-3′ (SEQ ID NO: 8) and 5′-TCGCATGATGATGACCAAGT-3′ (SEQ ID NO: 9)), which is amplified only in the presence of the Kinandang Patong-type DNA, and SNP02-IR64 (primers: 5′-ATCGTCTAGATCACGCAGTGAAC-3′ (SEQ ID NO: 10) and 5′-AGGGTGGCTTTACCTCCGTA-3′ (SEQ ID NO: 11)), which is amplified only in the presence of the IR64-type DNA.

[0360] The PCR mixture contained 0.2 μM primers, 0.6 U of Tag, 0.2 mM dNTPs, 2 mM MgCl.sub.2, and 20 ng of DNA per reaction (15 μL). The PCR reaction conditions were as follows: (1) 95° C. for 2 minutes; (2) 94° C. for 30 seconds; (3) annealing temperature ranging from 51.8 to 62.2° C. for 30 seconds; (4) 72° C. for 1 minute; and (5) for 7 minutes; 25 cycles of reactions (2) to (4) for SNP02-KP; 30 cycles of reactions (2) to (4) for SNP02-IR64. The PCR products were electrophoresed. The result showed that SNP02-KP was amplified only when using Kinandang Patong DNA, while SNP02-IR64 was amplified only when using IR64 DNA (FIG. 9).

INDUSTRIAL APPLICABILITY

[0361] The present invention provides the Dro1 gene, which controls the deep rooting of plants such as rice plants, and plants transformed with the gene. It is expected that plants with improved drought avoidance ability are produced by manipulating the Dro1 gene to convert a shallow-rooted plant into a deep-rooted plant. Alternatively, wet resistance can be conferred to plants by manipulating the Dro1 gene so that a deep-rooted plant is converted into a shallow-rooted plant.

[0362] Droughts have caused a serious reduction in the world crop yield. Meanwhile, in Japan, since paddy fields have poor drainage efficiency, wet damage has been problematic for soy and corn without wet resistance. The present invention is useful for solving such domestic and international problems.